Cargando…

Binary colloidal crystals (BCCs) as a feeder-free system to generate human induced pluripotent stem cells (hiPSCs)

Human induced pluripotent stem cells (hiPSCs) are capable of differentiating into any cell type and provide significant advances to cell therapy and regenerative medicine. However, the current protocol for hiPSC generation is relatively inefficient and often results in many partially reprogrammed co...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wang, Peng-Yuan, Hung, Sandy Shen-Chi, Thissen, Helmut, Kingshott, Peter, Wong, Raymond Ching-Bong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2016
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104981/ https://www.ncbi.nlm.nih.gov/pubmed/27833126 http://dx.doi.org/10.1038/srep36845

Ejemplares similares

Reprogramming of HUVECs into Induced Pluripotent Stem Cells (HiPSCs), Generation and Characterization of HiPSC-Derived Neurons and Astrocytes
por: Haile, Yohannes, et al.
Publicado: (2015)

Dopaminergic differentiation of schizophrenia hiPSCs
por: Hartley, Brigham J., et al.
Publicado: (2015)

Genetic Cardiomyopathies: The Lesson Learned from hiPSCs
por: My, Ilaria, et al.
Publicado: (2021)

The Role of MicroRNAs in Early Chondrogenesis of Human Induced Pluripotent Stem Cells (hiPSCs)
por: Stelcer, Ewelina, et al.
Publicado: (2019)

Generation of hiPSC-Derived Skeletal Muscle Cells: Exploiting the Potential of Skeletal Muscle-Derived hiPSCs
por: Metzler, Eric, et al.
Publicado: (2022)

Fluorescent Gene Tagging of Transcriptionally Silent Genes in hiPSCs
por: Roberts, Brock, et al.
Publicado: (2019)

hiPSCs for predictive modelling of neurodegenerative diseases: dreaming the possible
por: Rivetti di Val Cervo, Pia, et al.
Publicado: (2021)

Fabrication of functional ameloblasts from hiPSCs for dental application
por: Kim, Ka-Hwa, et al.
Publicado: (2023)

Platform for Induction and Maintenance of Transgene-free hiPSCs Resembling Ground State Pluripotent Stem Cells
por: Valamehr, Bahram, et al.
Publicado: (2014)

Analysis of Influenza A virus infection in human induced pluripotent stem cells (hiPSCs) and their derivatives
por: Ruangrung, Kanyarat, et al.
Publicado: (2022)

Organoid factory: The recent role of the human induced pluripotent stem cells (hiPSCs) in precision medicine
por: Novelli, Giuseppe, et al.
Publicado: (2023)

The translational potential of human induced pluripotent stem cells for clinical neurology: The translational potential of hiPSCs in neurology
por: Devine, Helen, et al.
Publicado: (2016)

ASSURED-optimized CRISPR protocol for knockout/SNP knockin in hiPSCs
por: Ludwik, Katarzyna A., et al.
Publicado: (2023)

A Defined, Feeder-Free, Serum-Free System to Generate In Vitro Hematopoietic Progenitors and Differentiated Blood Cells from hESCs and hiPSCs
por: Salvagiotto, Giorgia, et al.
Publicado: (2011)

Efficient Differentiation of Human Induced Pluripotent Stem Cell (hiPSC) Derived Hepatocyte-Like Cells on hMSCs Feeder
por: Mobarra, Naser, et al.
Publicado: (2014)

Comparison of Four Protocols to Generate Chondrocyte-Like Cells from Human Induced Pluripotent Stem Cells (hiPSCs)
por: Suchorska, Wiktoria Maria, et al.
Publicado: (2016)

Experimental Models to Study Autism Spectrum Disorders: hiPSCs, Rodents and Zebrafish
por: Pensado-López, Alba, et al.
Publicado: (2020)

Biomaterials and Advanced Biofabrication Techniques in hiPSCs Based Neuromyopathic Disease Modeling
por: Sun, Jing, et al.
Publicado: (2019)

Applying hiPSCs and Biomaterials Towards an Understanding and Treatment of Traumatic Brain Injury
por: Lacalle-Aurioles, María, et al.
Publicado: (2020)

PCSK9 regulates the NODAL signaling pathway and cellular proliferation in hiPSCs
por: Roudaut, Meryl, et al.
Publicado: (2021)

GCT-19. MODELING GERM CELL TUMORS WITH KIT MUTANT hiPSCs
por: Kuzuoka, Sakura, et al.
Publicado: (2020)

Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2
por: Spitalieri, Paola, et al.
Publicado: (2018)

Differentiation and Functional Comparison of Monocytes and Macrophages from hiPSCs with Peripheral Blood Derivatives
por: Cao, Xu, et al.
Publicado: (2019)

GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm
por: Sharma, Arun, et al.
Publicado: (2020)

Effects of Simulated Microgravity on Wild Type and Marfan hiPSCs-Derived Embryoid Bodies
por: Spitalieri, Paola, et al.
Publicado: (2021)

Microvessels derived from hiPSCs are a novel source for angiogenesis and tissue regeneration
por: Gao, Xin, et al.
Publicado: (2022)

Xeno-Free Integrated Platform for Robust Production of Cardiomyocyte Sheets from hiPSCs
por: Dias, Tiago P., et al.
Publicado: (2022)

Generation of hiPSCs with ABO c.767T>C substitution: resulting in splicing variants
por: Jin, Yinge, et al.
Publicado: (2023)

Understanding the molecular basis of autism in a dish using hiPSCs-derived neurons from ASD patients
por: Lim, Chae-Seok, et al.
Publicado: (2015)

Analysis of protein coding mutations in hiPSCs and their possible role during somatic cell reprogramming
por: Ruiz, Sergio, et al.
Publicado: (2013)

FUS Mislocalization and Vulnerability to DNA Damage in ALS Patients Derived hiPSCs and Aging Motoneurons
por: Higelin, Julia, et al.
Publicado: (2016)

PGC-1α promotes mitochondrial respiration and biogenesis during the differentiation of hiPSCs into cardiomyocytes
por: Zhou, Qin, et al.
Publicado: (2020)

Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives
por: Peron, Camille, et al.
Publicado: (2021)

Investigation of the hepatic development in the coculture of hiPSCs-derived LSECs and HLCs in a fluidic microenvironment
por: Danoy, Mathieu, et al.
Publicado: (2021)

CRISPR-Cas9 in hiPSCs: A new era in personalized treatment for Stargardt disease
por: Kuntam, Soujanya, et al.
Publicado: (2023)

Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview
por: Giovenale, Angela Maria Giada, et al.
Publicado: (2023)

Development of a protein marker panel for characterization of human induced pluripotent stem cells (hiPSCs) using global quantitative proteome analysis
por: Pripuzova, Natalia S., et al.
Publicado: (2015)

Aberrant hiPSCs-Derived from Human Keratinocytes Differentiates into 3D Retinal Organoids that Acquire Mature Photoreceptors
por: Shrestha, Rupendra, et al.
Publicado: (2019)

Optimized Surface Markers for the Prospective Isolation of High-Quality hiPSCs using Flow Cytometry Selection
por: Abujarour, Ramzey, et al.
Publicado: (2013)

Reproducible and efficient generation of functionally active neurons from human hiPSCs for preclinical disease modeling
por: Xie, Yunyao, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_v1na6rtifc79vp3cvoq2fava3n